Congenital stationary night blindness autosomal dominant 3

Definition

A congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the GNAT1 gene on chromosome 3p21.

Also known as congenital stationary night blindness autosomal dominant type 3, CSNBAD3, night blindness, congenital stationary, autosomal dominant type 3 — per MONDO

Also identified as

• DOID 0110715 per MONDO
• MESH C566475 per MONDO
• OMIM 610444 per MONDO
• UMLS C1864870 per MONDO